Detalhe da pesquisa
1.
Distinct roles of IL-18 and IL-1ß in murine model of macrophage activation syndrome.
J Allergy Clin Immunol
; 152(4): 940-948.e6, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37352976
2.
CD169 expression on monocytes as a marker for assessing type I interferon status in pediatric inflammatory diseases.
Clin Immunol
; 250: 109329, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37061149
3.
A Japanese Case of COVID-19 Caused by Omicron Strain with Y453F Substitution.
Rinsho Biseibutshu Jinsoku Shindan Kenkyukai Shi
; 33(1): 19-21, 2023 Dec 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38229458
4.
Progressive pulmonary fibrosis in a murine model of Hermansky-Pudlak syndrome.
Respir Res
; 23(1): 112, 2022 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35509004
5.
An atypical case of Kawasaki disease with severe pneumonia in a neonate.
BMC Pediatr
; 22(1): 132, 2022 03 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35287620
6.
Bi-allelic TMEM94 Truncating Variants Are Associated with Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial Dysmorphism.
Am J Hum Genet
; 103(6): 948-967, 2018 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30526868
7.
Serum insulin-like growth factor-binding protein 2 levels as an indicator for disease severity in enterohemorrhagic Escherichia coli induced hemolytic uremic syndrome.
Ren Fail
; 43(1): 382-387, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33641616
8.
Expanding the phenotype of COPA syndrome: a kindred with typical and atypical features.
J Med Genet
; 56(11): 778-782, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30385646
9.
ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
PLoS Genet
; 13(2): e1006481, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28158191
10.
Correction: ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
PLoS Genet
; 13(2): e1006624, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28241013
11.
Microangiopathic antiphospholipid antibody syndrome due to anti-phosphatidylserine/prothrombin complex IgM antibody.
Pediatr Int
; 59(3): 378-380, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28317300
12.
A Bladder Mass in a Patient with Henoch-Schönlein Purpura.
J Pediatr
; 231: 289-290, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33321145
13.
Recurrent painful ophthalmoplegic neuropathy.
J Paediatr Child Health
; 57(8): 1303-1304, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32870577
14.
Urinary neopterin: an immune activation marker in mesangial proliferative glomerulonephritis.
Clin Exp Nephrol
; 19(2): 264-70, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24858931
15.
Facial nerve palsy with splenomegaly.
J Paediatr Child Health
; 56(6): 974-975, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31850606
16.
Rotavirus gastroenteritis-associated urinary ammonium acid urate crystals.
Pediatr Int
; 57(1): 158-60, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25711254
17.
Case report: A family of atypical hemolytic uremic syndrome involving a CFH::CFHR1 fusion gene and CFHR3-1-4-2 gene duplication.
Front Immunol
; 15: 1360855, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38524137
18.
Distinct cytokine profile in juvenile systemic lupus erythematosus-associated macrophage activation syndrome.
Clin Immunol
; 146(2): 73-6, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23291246
19.
Cytokine profiles in children with primary Epstein-Barr virus infection.
Pediatr Blood Cancer
; 60(7): E46-8, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23382108
20.
Accumulation of mature B cells in the inflamed muscle tissue of a patient with anti-155/140 antibody-positive juvenile dermatomyositis.
Mod Rheumatol
; 23(1): 167-71, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22454192